Expression constructs and methods of genetically engineering methylotrophic yeast
Methods and materials for genetically engineering methylotrophic yeast are provided.
1. A methylotrophic yeast cell comprising a recombinant nucleic acid molecule, wherein the recombinant nucleic acid molecule comprises a first exogenous nucleic acid encoding a methanol expression regulator 1 (Mxr1) transcriptional activator operably linked to at least one methanol-inducible promoter element comprising a sequence to which the Mxr1 transcriptional activator binds, wherein the recombinant nucleic acid molecule comprises a second exogenous nucleic acid encoding a heterologous polypeptide operably linked to at least one methanol-inducible promoter element.
2. The yeast cell of claim 1 , wherein the methylotrophic yeast cell is of a yeast selected from the group consisting of Candida, Hansenula, Pichia and Torulopsis.
3. The yeast cell of claim 1 , wherein the cell is a Pichia cell.
4. The yeast cell of claim 1 , wherein the cell is a Pichia pastoris cell.
5. The yeast cell of claim 1 , wherein the recombinant nucleic acid molecule is stably integrated into the genome of the methylotrophic yeast cell.
6. The yeast cell of claim 1 , wherein the recombinant nucleic acid molecule is extrachromosomally expressed from a replication-competent plasmid.
7. The yeast cell of claim 1 , wherein the exogenous nucleic acid encoding a transcriptional activator comprises a Mxr1 sequence from Pichia pastoris.
8. The yeast cell of claim 1 , wherein the transcriptional activator comprises the sequence shown in SEQ ID NO: 59.
9. The yeast cell of claim 8 , wherein the transcriptional activator is encoded by the nucleic acid sequence shown in SEQ ID NO: 60.
10. The yeast cell of claim 1 , wherein the at least one methanol-inducible promoter element is selected from the group consisting of an alcohol oxidase 1 (AOX1) promoter element from Pichia pastoris , an alcohol oxidase (AOD1) promoter element from Candida boidinii , a methanol oxidase (MOX) promoter element from Hansenula polymorpha , a methanolica alcohol oxidase (MOD1) promoter element from Pichia methanolica , a dihydroxyacetone synthase (DHAS) promoter element from Pichia pastoris , a formaldehyde dehydrogenase (FLD1) promoter element from Pichia pastoris , and a peroxin 8 (PEX8) promoter element from Pichia pastoris.
11. The yeast cell of claim 1 , wherein the at least one methanol-inducible promoter element is an alcohol oxidase 1 (AOX1) promoter element from Pichia pastoris.
12. The yeast cell of claim 1 , wherein the second exogenous nucleic acid encodes at least one heterologous polypeptide involved in biosynthesis of an iron co-factor.
13. The yeast cell of claim 12 , wherein the iron co-factor is heme.
14. The yeast cell of claim 13 , wherein the at least one polypeptide involved in the biosynthesis of heme is selected from the group consisting of aminolevulinic acid (ALA) synthase, ALA dehydratase, porphobilinogen deaminase, uroporphyrinogen (UPG) III synthase, UPG III decarboxylase, coproporphyrinogen (CPG) oxidase, protoporphyrin (PPG) oxidase, and ferrochelatase.
15. The yeast cell of claim 13 , wherein the at least one polypeptide involved in the biosynthesis of heme comprises two or more polypeptides selected from the group consisting of ALA synthase, ALA dehydratase, porphobilinogen deaminase, UPG III synthase, UPG III decarboxylase, CPG oxidase, PPG oxidase, and ferrochelatase.
16. A method for expressing a heterologous polypeptide in a cell, the method comprising:
providing the yeast cell of claim 1 ; and
culturing the cell under conditions for expression of the recombinant nucleic acid molecule,
thereby expressing the heterologous polypeptide.
17. The method of claim 16 , wherein the heterologous polypeptide is a member of globin family PF00042.
18. The method of claim 16 , wherein the heterologous polypeptide is a plant hemoglobin.
19. The method of claim 18 , wherein the plant hemoglobin is leghemoglobin.
20. The method of claim 19 , wherein the leghemoglobin has a sequence selected from the group consisting of SEQ ID NO:4 and SEQ ID NO:6.
21. The method of claim 16 , wherein the introducing step comprises a technique selected from the group consisting of transduction, electroporation, biolistic particle delivery, and chemical transformation.
22. The method of claim 16 , wherein the conditions under which the cell is cultured comprises addition of iron or a pharmaceutically or metabolically acceptable salt thereof.
23. The method of claim 16 , wherein the culturing step comprises culturing the cell in the presence of methanol.
24. The method of claim 16 , wherein the culturing step comprises culturing the cell in the absence of methanol.
25. The method of claim 16 , wherein the culturing step comprises culturing the cell in the absence of selection.
26. A methylotrophic Pichia yeast cell comprising a recombinant nucleic acid molecule, wherein the recombinant nucleic acid molecule comprises:
a nucleic acid encoding a Mxr1 transcriptional activator sequence from P. pastoris;
a nucleic acid encoding a member of globin family PF00042; and a nucleic acid encoding at least one polypeptide involved in heme biosynthesis, wherein each nucleic acid is operably linked to a methanol-inducible promoter element, wherein the methanol-inducible promoter element comprises at least one sequence to which a Mxrl1 transcriptional activator binds.
27. The yeast cell of claim 26 , wherein the member of the globin family is leghemoglobin.
28. The yeast cell of claim 26 , wherein the methanol-inducible promoter element is an alcohol oxidase 1 (AOX1) promoter element from P. pastoris.